US3256167A - Process for j,x,s,g,-tetrachloro-z-(trichloromethyl) pyridine composition - Google Patents
Process for j,x,s,g,-tetrachloro-z-(trichloromethyl) pyridine composition Download PDFInfo
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- US3256167A US3256167A US3256167DA US3256167A US 3256167 A US3256167 A US 3256167A US 3256167D A US3256167D A US 3256167DA US 3256167 A US3256167 A US 3256167A
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- United States
- Prior art keywords
- picoline
- reactor
- pyridine
- chlorine
- trichloromethyl
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 216
- 238000000034 method Methods 0.000 title claims description 64
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title description 44
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-Methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims description 158
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 152
- 239000000460 chlorine Substances 0.000 claims description 112
- 229910052801 chlorine Inorganic materials 0.000 claims description 110
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 110
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 98
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 98
- 239000007788 liquid Substances 0.000 claims description 96
- 239000007791 liquid phase Substances 0.000 claims description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 239000000047 product Substances 0.000 description 94
- YMBFWRZKTZICHS-UHFFFAOYSA-N 2,3,4,5-tetrachloro-6-(trichloromethyl)pyridine Chemical compound ClC1=NC(C(Cl)(Cl)Cl)=C(Cl)C(Cl)=C1Cl YMBFWRZKTZICHS-UHFFFAOYSA-N 0.000 description 54
- OMSBSIXAZZRIRW-UHFFFAOYSA-N 2-methylpyridine;hydrochloride Chemical compound Cl.CC1=CC=CC=N1 OMSBSIXAZZRIRW-UHFFFAOYSA-N 0.000 description 54
- 238000006243 chemical reaction Methods 0.000 description 50
- 238000002360 preparation method Methods 0.000 description 28
- 239000003054 catalyst Substances 0.000 description 26
- 238000005660 chlorination reaction Methods 0.000 description 22
- 239000007789 gas Substances 0.000 description 22
- 239000011541 reaction mixture Substances 0.000 description 20
- 239000007787 solid Substances 0.000 description 20
- ISJBPOYWLKRORP-UHFFFAOYSA-N 3,4,5-trichloro-2-(dichloromethyl)pyridine Chemical compound ClC(Cl)C1=NC=C(Cl)C(Cl)=C1Cl ISJBPOYWLKRORP-UHFFFAOYSA-N 0.000 description 16
- 238000001816 cooling Methods 0.000 description 16
- 239000000463 material Substances 0.000 description 16
- 238000010924 continuous production Methods 0.000 description 14
- 239000003999 initiator Substances 0.000 description 14
- YWSFDYUMEBEQNZ-UHFFFAOYSA-N 3,4,5-trichloro-2-(trichloromethyl)pyridine Chemical compound ClC1=CN=C(C(Cl)(Cl)Cl)C(Cl)=C1Cl YWSFDYUMEBEQNZ-UHFFFAOYSA-N 0.000 description 12
- VSCWAEJMTAWNJL-UHFFFAOYSA-K Aluminium chloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 12
- 238000005755 formation reaction Methods 0.000 description 12
- 239000011968 lewis acid catalyst Substances 0.000 description 12
- 239000006227 byproduct Substances 0.000 description 10
- KZBUYRJDOAKODT-UHFFFAOYSA-N chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 10
- 238000010521 absorption reaction Methods 0.000 description 8
- 238000004508 fractional distillation Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- KAQJMEHRXVENSF-UHFFFAOYSA-N 2-(trichloromethyl)pyridine Chemical class ClC(Cl)(Cl)C1=CC=CC=N1 KAQJMEHRXVENSF-UHFFFAOYSA-N 0.000 description 6
- MEQBJJUWDCYIAB-UHFFFAOYSA-N 2-chloropyridin-3-amine Chemical class NC1=CC=CN=C1Cl MEQBJJUWDCYIAB-UHFFFAOYSA-N 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 238000004587 chromatography analysis Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000011065 in-situ storage Methods 0.000 description 6
- 239000000543 intermediate Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 230000000361 pesticidal Effects 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N Carbon tetrachloride Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- RBTARNINKXHZNM-UHFFFAOYSA-K Iron(III) chloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 4
- UHZYTMXLRWXGPK-UHFFFAOYSA-N Phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N Thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 229910001510 metal chloride Inorganic materials 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000006011 modification reaction Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- MSRGJVQTGNSQOZ-UHFFFAOYSA-N 2,3,5-trichloro-6-(trichloromethyl)pyridine Chemical compound ClC1=CC(Cl)=C(C(Cl)(Cl)Cl)N=C1Cl MSRGJVQTGNSQOZ-UHFFFAOYSA-N 0.000 description 2
- YHPMRWZVIQTSFZ-UHFFFAOYSA-N 3,5-difluoro-2-(2-fluorophenyl)pyridine Chemical compound FC1=CC(F)=CN=C1C1=CC=CC=C1F YHPMRWZVIQTSFZ-UHFFFAOYSA-N 0.000 description 2
- XAYLRCRXDBZOBH-UHFFFAOYSA-N 3-chloro-2-(trichloromethyl)pyridine Chemical compound ClC1=CC=CN=C1C(Cl)(Cl)Cl XAYLRCRXDBZOBH-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 240000001592 Amaranthus caudatus Species 0.000 description 2
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 2
- 240000007528 Amaranthus viridis Species 0.000 description 2
- 235000004135 Amaranthus viridis Nutrition 0.000 description 2
- FAPDDOBMIUGHIN-UHFFFAOYSA-K Antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 description 2
- 241001124076 Aphididae Species 0.000 description 2
- 241001674044 Blattodea Species 0.000 description 2
- 235000009344 Chenopodium album Nutrition 0.000 description 2
- 235000005484 Chenopodium berlandieri Nutrition 0.000 description 2
- 235000009332 Chenopodium rubrum Nutrition 0.000 description 2
- QPUXSGYGSMOSCT-UHFFFAOYSA-N ClCC=1C(=NC(=C(C1CCl)CCl)CCl)C(Cl)(Cl)Cl Chemical compound ClCC=1C(=NC(=C(C1CCl)CCl)CCl)C(Cl)(Cl)Cl QPUXSGYGSMOSCT-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- MPCRDALPQLDDFX-UHFFFAOYSA-L Magnesium perchlorate Chemical compound [Mg+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O MPCRDALPQLDDFX-UHFFFAOYSA-L 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- 240000005158 Phaseolus vulgaris Species 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- FAIAAWCVCHQXDN-UHFFFAOYSA-N Phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 2
- YBBRCQOCSYXUOC-UHFFFAOYSA-N Sulfuryl chloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J Tin(IV) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- CBWUNQZJGJFJLZ-UHFFFAOYSA-N [Cl].Cl Chemical compound [Cl].Cl CBWUNQZJGJFJLZ-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 230000000240 adjuvant Effects 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000005587 bubbling Effects 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L cacl2 Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 230000003197 catalytic Effects 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 230000001419 dependent Effects 0.000 description 2
- 230000001627 detrimental Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000001586 eradicative Effects 0.000 description 2
- -1 for example Chemical class 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000008241 heterogeneous mixture Substances 0.000 description 2
- 239000008240 homogeneous mixture Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000011344 liquid material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 230000000717 retained Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000009738 saturating Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Definitions
- This invention relates to chlorination and more particularly to methods for selectively preparing certain highly chlorinated picoline compounds.
- Certain highly chlorinated picoline compounds are useful as pesticides or as intermediates for the preparation
- known methods of chlorination have provided such complex mixtures and low yields of the various components as to render such methods unsuitable as synthetic methods for the preparation of a particular component or group of components.
- chlorination of picolines has been carried out in the presence of water whereby a spectrum of chlorination products have been obtained, none in significant amounts.
- certain of the components obtained by this method may be recovered by fractional distillation, because of the uncontrollability of the process for selective preparation of products, the actual amount of one or of even several of the components taken together have been so small as to render the method inoperative for preparative purposes.
- the other known procedure for chlorination of picolines employs the step of saturating liquid picoline with hydrogen chloride whereupon'a heterogeneous mixture containing solid picoline hydrochloride in picoline is formed and thereafter passing gaseous chlorine through the mixture for a long period to effect a reaction as evidenced by the disappearance of the solid and formation of a relatively homogeneous mixture.
- This procedure has produced a wide range of chlorinated products and a great deal of tarry materials and although some of the components have been recoverable by fractional distillation, the amount of any particular product or group of products has been small.
- the previous method has not been employable as a reproduceable method for the production of selected chlorinated picoline product or a group of products.
- high yields of highly chlorinated materials may be prepared in a continuous process. More particularly, it has been discovered that good yields of highly chlorinated picoline compounds wherein the product is enriched in 3,4,5 ,6-tetrachloro-2-(trichloromethyl)pyridine may be prepared by a continuous low temperature chlorination process as hereinafter described.
- the product mixture contains 'two other-highly chlorinated picolines in significant but readily separable amounts and which is substantially free of isomeric contaminants, lower chlorinated materials and decompositions products.
- a product composition which is enriched in 3,4,5,6-tetrachloromethyl-2-(trichloromethyl)pyridine and which contains 3,4,S-trichloro-2-(trichloromethyDpyridine and 3,4,5-trichloro-2- (dichloromethyl) pyridine as the other major components. It is significant that not only does the present process permit the preparation of the desired components in good yields and in a form readily separable from the minor amounts of lower chlorinated byproducts, but that the by-products are free from tarry decomposition products, permitting their use as starting materials for the preparation of other chemical intermediates and ultimate chemical products.
- the present process also provides for the first time, a method which is feasible as a preparative line mixture available as initiator charge.
- chlorination of a-picoline may be carried out rapidly and economically and with the production of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine in a process which comprises introducing a-picoline and gaseous chlorine continuously and simultaneously at points substantially removed from one another into a reaction system whereby a reaction takes place in the liquid phase to form the desired product mixture enriched in 3,4,5,6-tetrachloro-2- (trichloromethyl) pyridine.
- picoline when the expression picoline is employed, it will be intended to designate fa-picoline.
- liquid picoline hydrochloride composition a homogeneous liquid mixture or solution which results when picoline hydrochloride which is normally a solid is brought into contact with excess hydrogen chloride gas.
- chlorine gas is introduced into an appropriate, heated liquid system comprising an initiator charge, as hereinafter described, to produce hydrogen chloride gas in situ which is conducted therefrom to a cooled system and contacted with picoline in a counter-current flow to form a liquid'picoline hydrochloride composition which is returned to the heated liquid system whereupon it reacts with gaseous chlorine to produce the desired product composition enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine.
- the initiator charge which is placed in the primary reactor to initiate the process of the present invention is defined as a liquid material which when contacted with gaseous chlorine reacts to produce hydrogen chloride.
- picoline charge and the recommended materials are chlorinated picoline mixture, preferably, a highly chlorinated picoline composition particularly of density 1.651.8. Such material would still contain reactable hydrogen but would avoid intro duction of foreign matter.
- chlorinated pico- If no chlorinated picoline is available, a small amount of picoline diluted with an inert low boiling solvent may be employed, the solvent being readily removable from the product after recovery thereof. Introduction of several equivalents of anhydrous HCl prior to chlorine introduction is necessary in this case. Otherwise solid picoline monohydrochloride which is detrimental to good yields contemplated by the process of this invention will form.
- the hydrogen chloride formed in situ is conducted to a cooled secondary reactor where under controlled temperated conditions it is contacted with picoline in an atmosphere of excess hydrogen chloride to form liquid picoline hydrochloride composition.
- picoline hydrochloride is formed but in the presence of excess hydrogen chloride, a liquid composition is formed.
- an efiicient means for contacting hydrogen chloride and picoline is in a counter-current flow relationship and the smooth conduction of the resulting material to the primary reactor is achieved by down-flow of a liquid composition.
- the desired results are achieved by controlling the temperatures in such a manner that a significant proportion of the initial heat of reaction between picoline and hydrogen chloride is removed but wherein a sufficiency of heat is retained to permit the formation of a liquid composition and to maintain the composition in a liquid state along the down-flow path to the primary reactor.
- Achievement of desired temperature control is best accomplished by employing a reactorof such shape and/ or dimensions as to provide a high degree of positive temperature control throughout the reactor.
- a reactorof such shape and/ or dimensions as to provide a high degree of positive temperature control throughout the reactor.
- a suitable temperature range for carrying out this step is from about 20 to about 70 C.
- the exact rate of introduction of chlorine into the primary reactor depends on the particular size of operation, shape of reactor, Whether or not mechanical mixing is employed, etc. For efiicient operation of this process, it is important that about 80 to 85 percent molar excess of chlorine be present at all times in the reactor to assure not only a rapid conversion of the reactant picolinehydrochloride material but also to continuously sweep out hydrogen chloride from the reactor.
- the desirablerate may be expressed in terms of the rate of introduction of the reactant picoline into the reaction system. Such rate is considered to be a ratioof chlorine to picoline of from about 11.521 to about 21.5:1 on weight basis.
- Illustrative of a desirable rate is-that of from-about 4 to 6 pounds of chlorine per hour at a picoline feed rate of 0.28 to 0.35 pounds per hour when introducedinto a, 6.4 gallon reactor containing about 4.5 gallons of reaction mixture.
- residence time is dependent on volume of reaction mixture and picoline feed rate necessary to hold a st ady state.
- steady state is meant the condition attained when the composition of the reaction mixture is no longer changing significantly.
- the time necessary to achieve a steady state depends on conditions applied to the system andis readily determined by .the skilled in the art.
- the density of the reaction mixture at steady state is from about 10 to 12 pounds per gallon, the averagefigure being about 11 pounds per gallon. It is to be noted that this density is an average density of the overall mixture in the reactor inasmuch as there develops as the reaction approaches a steady state, a dual liquid phase system of substantially definite proportions and having the above average densities.
- the upper liquid phase is a liquid hydrochloride composition comprising picoline hydrochloride and lower chlorinated picoline hydrochloride in excess hydrogen chloride, and the lower liquid phase comprises a highly chlorinated mixture enriched in 3,4,5,6-tetra-.
- the reaction may be carried out in the presence or absence of a catalytic light source.
- a catalytic light source The use of irradiation is considered preferable.
- a light source emitting light at a wave length of from about 2000 A. to 5000 A. and particularly between about 3000 A. to about 4000 A. are suitable.
- the light source may double as a source of heat.
- the reaction may be carried out in the presence or absence of a catalyst.
- a mixture enriched in highly chlorinated picoline compounds, particularly in 3,4,5,6- tetrachloro 2 (trichlorornethyl) pyridine is obtained in good yields in the absence of catalyst; this is noted particularly when product composition obtained by this method is compared with products obtained by using known chlorination methods. .However, it has been found that by using Lewis acid catalysts in the present process, the yield of the desired product composition is significantly increased; thus, the preferred method for preparing a mixture enriched in 3,4,5,6 tetrachloro-2-(trichloromethyl) pyridine contemplates the use of a Lewis acid catalyst. Any Lewis acid catalysts as understood in the art may be employed.
- Aluminum chloride phosphorus trichloride and ferric chloride.
- Others include stannic chloride, antimony trichloride, thionyl chloride, sulfuryl chloride, phosphorouspentachloride, calcium chloride, iodine, red phosphorus, etc.
- Lower valent salts of multi-valent metals as well as free metals may be employed. The latter when employed is readily converted by the hydrogen chloride formed in the reaction mixture to the corresponding metal chloride.
- the catalyst may be added in any amount up to 5 percent by weight of the picoline feed. Preferred amounts are from 0.5 to 1 percent by weight.
- the mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine thus obtained is water-white in color, has a substantially constant density, contains only minor proportions of lower chlorinated picolines and is substantially free of hydrogen chloride.
- This enriched product mixture forms a lower liquid phase in the reactor while the less chlorinated picoline dissolved in hydrogen chloride forms the less dense upper liquid phase.
- the exact composition of the product mixture to be removed from the reactor at the steady state may be determinedby vapor phase chromatographic analysis of samples or may be estimated by density comparison with a predetermined density-composition correlation.
- the average densities of the product enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, containing 3,4,5-trichloro-2-(trichloromethyl)pyridine and 3,4,5-trichloro-2-(dichloromethyl) pyridine as the major components vary from 1. 68 to 1.78,
- the product may be bled from the reactor by conventional methods and may be separated into its components, if desired, by fractional distillation.
- the apparatus comprises primarily of primary reactor A, reactor B, condenser C, hydrogen chloride absorption column D, chlorine drier E and gas shunting device F.
- Reactor A is the primary reactor to be employed as a liquid phase chlorinator; it is fitted with temperature control means a for heating or cooling and optionally with dimensions of reactor B are not important but must be such as to provide sufiicient cooling to prevent by-product formation but without excessive cooling as to cause separation of solid picoline hydrochloride. Good results have been obtained when the diameterzlength ratio was about 1:18 and tap water used for cooling.
- Condenser C has for its primary purpose avoidance of entrainment losses of reactant or product with effluent gases; it is fitted with cooling means d.
- Example 1 An operation was carried out in an apparatus having a schematic arrangement set forth in the accompanying drawing wherein reactor A was a vessel of 17 liter capacity and illuminated with ultraviolet light, reactor 13 was a water-cooled column 2 inches in internal diameter and 36 inches in length, a condenser C was a water-cooled column 2 inches in diameter and 14 inches in length.
- the hydrogen chloride absorption column D is a means for removing hydrogen chloride from the mixed chlorine-hydrogen chloride gases; it consists of downflowing water which meets the gases in counter-current relationship and aqueous hydrochloric acid is recovered at the bottom of the column.
- Chlorine drier B may be any suitable means for drying chlorine gas, a packed silica gel column being convenient; it is not by any means limited thereto and any device adapted to remove entrained water from chlorine using suitable dessicant such as sulfuric acid or magnesium perchlorate may be employed.
- a chlorine drier is of utmost importance in use of recycled chlorine inasmuch as the method of the present invention is carried out under substantially anhydrous conditions in contrast' to a single flow system.
- an initiator charge is placed in reactor A.
- Chlorine gas is introduced into the thus charged reactor A at 1 whereupon a reaction takes place with the evolution of hydrogen chloride gas-which leaves the reactor through inlet-outlet 2 and proceeds upward through orifice 4 into reactor B.
- Picoline is introduced at inlet 6 where it proceeds by gravity fiow into cooled reactor B, meeting the hydrogen chloride in a counter-current flow relationship and reacting on the walls thereof to form picoline hydrochloride which in the presence of excess hydrogen chloride is converted into a liquid picoline hydrochloride composition.
- the picoline thus introduced, contacted hydrogen chloride gas in a counter-current flow relationship and reacted therewith forming picoline hydrochloride which in the presence of excess hydrogen chloride gas formed a liquid picoline hydrochloride composition which proceeded downward into the primary reactor.
- 0.5 pound of aluminum chloride catalyst (about 1 percent by weight based on the total picoline used) was introduced at inlet 3. The catalyst came into contact with the liquid picoline'hydrochlorine composition leaving reactor B and was carried therewith into reactor A.
- the liquid picoline hydrochloride composition thus continuously introduced into the chlorination medium of reactor A, reacted with gaseous chlorine which was continuously introduced over a period of 72 hours to produce a product mixture enriched in 3,4,5,6- tetrachloro-Z-(trichloromethyl)pyridine.
- the product mixture was continuously removed from the reactor at 7 and amounted to 130 pounds.
- Vapor phase chromatographic analysis of the product mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl) pyridine showed the mixture to contain in adtion remains homogeneous and continues smoothly without the separation of solid picoline hydrochloride on the walls of the apparatus.
- the liquid picoline hydrochloride composition enters reactor A where, in the liquid phase and under controlled temperature conditions, it reacts with gaseous chlorine to produce the desired product mixture of chlorinated picolines enriched in 3,4,5,6-tetrachloro-2 (trichloromethyl) pyridine which may be recovered at 7.
- Hydrogen chloride, chlorine gas and entrained liquids proceed from reactor B to condenser C where the entrained liquids are separated from the gases by condensation and returned to reactor B.
- the gases proceed from the condenser to absorption column D where the gases meet down-flowing water in a counter-current relationship and wherein hydrogen chloride dissolves in the water forming hydrochloric acid which is recovered at 8.
- the gaseous chlorine proceeds from the absorption column at 9 and proceeds to chlorine drier E.
- the chlorine after passing through drying column B is joined at F with fresh chlorine and recycled through the reactor system.
- the catalyst When the process of the present invention is carried out in the presence of a catalyst, the catalyst may be introduced at inlet 3,'whereby it is conveyed into reactor A through inlet-outlet 2.
- the catalyst may be added condition 3,4,5-trichloro-2-(trichloromethyDpyridine and 3, 4,5-trichloro-2-(dichloromethyl)pyridine as major components.
- the product composition in mole percent wasas follows: 30 percent 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 32 percent 3,-4,5-trichloro-2-(trichloromethyl)pyridine, 16 percent 3,4,5-trichloro-2-(dichloromethyl)pyridine, about 6 percent 3,5-dichl0ro-2-(trichloromethyl) pyridine, about 7 percent 3,5,6-trichloro-2-(trichloromethyl) pyridine and about 4 percent 3,5-dichloro- Z-(dichloromethyl)pyridine.
- reaction mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, i.e., mixture containing primarily 3,4,5, 6- tetrachloro-2-(trichloromethyl)pyridine, 3,4,5-trichloro-2- trichloromethyl) pyridine and 3,4,5-trichloro-2-(dichloromethyl)pyridine, it is found that the lower chlorinated products distill ofl? in the forerun, 3,4,5-trichloro-2-(dichloromethyl) pyridine distills at from to C.
- Example 2 A reaction was carried out in a manner substantially as I percent troduced in the form of aluminum turnings, said aluminum reacting with the hydrogen chloride evolved from reactor A to form aluminum chloride in situ.
- This modified procedure there was obtained 32 mole percent 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 30 mole 3,4,5-trichloro-2-(trichloromethyl)pyridine and 15 mole percent 3,4,5-trichloro-2-(dichloromethyl)pyridine.
- Example 3 A similar operation was carried out in which the following modifications were made (a) change in rate of introduction of picoline to 250 grams per hour, (b) dark reaction, i.e., ultraviolet light was not employed, and (c) change in amount of catalyst employed (2 percent by weight of aluminum based on weight of picoline used). In a manner previously described, the chlorination was allowed to proceed for 40 hours to obtain a product mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl) pyridine which was continuously recovered from the reactor.
- Vapor phase chromatographic analysis of the product mixture showed 29 mole percent of 3,'4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 33 mole percent of 3,4,5-trichloro-2-(trichloromethyl)pyridine and 15 mole percent of 3,4,5-trichloro-2-(dichloromethyl) pyridine.
- Example 4 In another similar operation, an irradiated chlorination was carried out wherein ferric chloride catalyst, introduced as metallic iron in an amount of 1.5 percent by weight of picoline, was employed.
- the reaction was carried out in a manner as previously described by introducing chlorine gas into reactor A charged with a partially chlorinated picoline mixture and introducing picoline into reactor B at a rate of 250 grams per hour for 24 hours to obtain a highly chlorinated product composition containing 29 mole percent 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 32 mole percent 3,4,5-trichloro-2-(trichlorornethyl) pyridine and 17 mole percent 3,4,5-trichloro-2- dichlorornethyl) pyridine.
- the process of the present invention produces a very highly useful product composition which may be employed without change or may be separated into major components for ultimate use in product compositions or as starting materials for the preparation of other desirable products.
- the 3,4,5,6 tetrachloro 2 (trichloromethyl)pyridine enriched product may be diluted with inert adjuvants to obtain pesticidal treating compositions.
- the product is mixed with dispersing agents and dispersed in water to obtain spray compositions which when applied to foliage of bean, pigweed and foxtail plants effect complete kills of said plants.
- the 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine enriched product may be distilled to recover 3,4,5,6- tetrachloro-Z-(trichloromethyl)pyridine or 3,4,5-trichloro-2-(trichloromethyl)pyridine which may separately be employed in pesticidal compositions.
- the product mixture may also be distilled to recover the components which may be employed as intermediates in the preparation of other chemical compounds, such as for example, aminochloropyridine compounds by heating the recovered component with liquid ammonia in a sealed vessel at temperatures of from about 70 to above 190 C. at autogeneous pressure.
- the resulting aminochloropyridine compounds may be employed for the control of insect pests such as house-fly, cockroach, mites, aphids, etc. or for the eradication of weeds or weed seeds.
- the aminochloropyridine compounds may be prepared with dispersing agents to form aqueous dispersion or dispersed on inert solids to form dust compositions to be applied to infested areas.
- a process for preparing a mixture enriched in 3,4.5,6 tetrachloro 2 (trichloromethyl) pyridine which comprises (1) contacting (X-PiCOline and hydrogen chloride in a cooled reactor at temperatures in the range of from about 20 C. to about 70 C. to produce a liquid tx-picoline hydrochloride composition,
- the chlorine and OL- picoline are introduced in a ratio of chlorine to picoline of from about 11.511 to about 21.5:1 on a weight basis.
- a process for preparing a mixture enriched in 3,4,5,6 tetrachloro 2 (trichloromethyl)pyri-dine which comprises (1) contacting LZ-PiCOiine and hydrogen chloride at temperatures in the range of from about 20 C. to 70 C. to produce a liquid a-picoline hydrochloride composition,
- the chlorine and a-picoline are introduced in a ratio of chlorine to picoline of from about ll.5:1 to 21.5:1 on a weight basis.
- step (2) is carried out while the mixture is irradiated with actinic radiation.
- step (2) is carried out in the presence of a Lewis acid catalyst.
- step (2) is carried out in the presence of Lewis catalyst and actinic radiation.
- a continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichlorornethyl)- pyridine which comprises (1) continuously feeding tat-picoline into a cooled reactor,
- the chlorine and apicoline are introduced in a ratio of chlorine to picoline of from about 11.5:1 to about 21.5:1 on a weight basis.
- a continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)- pyridine which comprises (1) charging a heated reactor with a picoline charge,
- the chlorine and apicoline are introduced in a ratio of chlorine to picoline of from about 11.5 :1 to about 21.5 :1 on a weight basis.
- a continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)- pyridine which comprises 1) charging a heated reactor with a picoline charge comprising chlorinated picolines having a density of from about 1.65 to 1.8,
- the chlorine and apicoline are introduced in a ratio of chlorine to picoline of from about 11.5:1 to about 21.5:1 on a weight basis.
- a process for preparing a mixture enriched in 3,4,5,6 tetrachloro 2-(trichloromethyl)pyridine which comprises (1) contacting a-picoline and hydrogen chloride in a cooled reactor at temperatures in the range of from about 20 C. to about 70 C. to produce a liquid orpicoline hydrochloride composition,
- the rate of introduction of chlorine into the reactor is such as to provide therefor its presence therein throughout the reaction in about 80 to 85 percent molar excess on a stoichiometric basis.
- a process for preparing a mixture enriched in 3,4,5,6 tetrachloro '2-(trich-loromethyl)pyridine which comprises i (1) contacting a-picoline and hydrogen chloride at temperatures in the range of from about 20 C. to about 70 C. to produce a liquid a-picoline hydrochloride composition,
- the rate of introduction of chlorine into the retactor is such as to provide for its presence therein throughout the reaction in about 80 to 85 percent molar excess on a stoichiomet-ric basis.
- step (2) is carried out while the mixture is irradiated with actinic radiation.
- step (2) is carried out in the presence of a Lewis acid catalyst.
- step (2) is carried out in the presence or Lewis acid catalyst and actinic radiation.
- a continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichlorome-thyl) pyridine which comprises (1) continuously feeding a-picoline into a cooled r actor, I
- the rate of introduction of chlorine into the reactor is such as to provide for its presence therein throughout the reaction in about to percent molar excess on a stoichiometric basis.
- a continuous process for the preparation of a mixture enriched in 3,4,5,6 -tetrachloro-2-(trichloromethyl)pyridine which comprises (1) charging a heated reactor with a picoline charge,
- the rate'of introduction of chlorine into the reactor is such as to provide for its presence therein throughout the reaction in about 80 to 85 percent molar excess on a stoichiometric basis.
- a continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyDpy ridine which comprises (1) charging a heated reactor with a picoline charge comprising chlorinated picolines having a density of from about 1.65 to 1.8,
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Description
of other compounds having pesticidal properties.
United States Patent 3,256,167 PROCESS FOR 3,4,5,6-TETRACHLORO-2-(TRI- CHLOROMETHYDPYRIDINE COMPOSITION Frederick H. Norton and William H. T aplin Ill, Concord,
Califi, assiguors to The Dow Chemical Company, Midland, Micl1., a corporation of Delaware Filed Mar. 6, 1962, Ser. No. 177,871 16 Claims. (Cl. 204- -158) This invention relates to chlorination and more particularly to methods for selectively preparing certain highly chlorinated picoline compounds.
Certain highly chlorinated picoline compounds are useful as pesticides or as intermediates for the preparation However, known methods of chlorination have provided such complex mixtures and low yields of the various components as to render such methods unsuitable as synthetic methods for the preparation of a particular component or group of components. Thus, chlorination of picolines has been carried out in the presence of water whereby a spectrum of chlorination products have been obtained, none in significant amounts. Although certain of the components obtained by this method may be recovered by fractional distillation, because of the uncontrollability of the process for selective preparation of products, the actual amount of one or of even several of the components taken together have been so small as to render the method inoperative for preparative purposes. The other known procedure for chlorination of picolines employs the step of saturating liquid picoline with hydrogen chloride whereupon'a heterogeneous mixture containing solid picoline hydrochloride in picoline is formed and thereafter passing gaseous chlorine through the mixture for a long period to effect a reaction as evidenced by the disappearance of the solid and formation of a relatively homogeneous mixture. This procedure has produced a wide range of chlorinated products and a great deal of tarry materials and although some of the components have been recoverable by fractional distillation, the amount of any particular product or group of products has been small. Thus, as with the previous method, has not been employable as a reproduceable method for the production of selected chlorinated picoline product or a group of products.
According to the present invention, it has been discovered that high yields of highly chlorinated materials may be prepared in a continuous process. More particularly, it has been discovered that good yields of highly chlorinated picoline compounds wherein the product is enriched in 3,4,5 ,6-tetrachloro-2-(trichloromethyl)pyridine may be prepared by a continuous low temperature chlorination process as hereinafter described. The product mixture contains 'two other-highly chlorinated picolines in significant but readily separable amounts and which is substantially free of isomeric contaminants, lower chlorinated materials and decompositions products. By carrying out the process of the present invention, a product composition, is obtained which is enriched in 3,4,5,6-tetrachloromethyl-2-(trichloromethyl)pyridine and which contains 3,4,S-trichloro-2-(trichloromethyDpyridine and 3,4,5-trichloro-2- (dichloromethyl) pyridine as the other major components. It is significant that not only does the present process permit the preparation of the desired components in good yields and in a form readily separable from the minor amounts of lower chlorinated byproducts, but that the by-products are free from tarry decomposition products, permitting their use as starting materials for the preparation of other chemical intermediates and ultimate chemical products. The present process also provides for the first time, a method which is feasible as a preparative line mixture available as initiator charge.
method for highly chlorinated (trichloromethyl)pyridine ice compounds, and which furthermore is a feasible commercial production method.
It has been discovered that chlorination of a-picoline may be carried out rapidly and economically and with the production of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine in a process which comprises introducing a-picoline and gaseous chlorine continuously and simultaneously at points substantially removed from one another into a reaction system whereby a reaction takes place in the liquid phase to form the desired product mixture enriched in 3,4,5,6-tetrachloro-2- (trichloromethyl) pyridine. Hereinafter, when the expression picoline is employed, it will be intended to designate fa-picoline. The process involves first forming a liquid picoline hydrochloride composition, introducing the composition into a liquid phase system, bubbling gaseous chlorine through the liquid phase system under controlled temperature conditions to produce the desired mixture enriched in 3,4,5,6-tetrachloro-2-(trichl'oromethyl)pyridine. By liquid picoline hydrochloride composition is meant a homogeneous liquid mixture or solution which results when picoline hydrochloride which is normally a solid is brought into contact with excess hydrogen chloride gas. In this process, chlorine gas is introduced into an appropriate, heated liquid system comprising an initiator charge, as hereinafter described, to produce hydrogen chloride gas in situ which is conducted therefrom to a cooled system and contacted with picoline in a counter-current flow to form a liquid'picoline hydrochloride composition which is returned to the heated liquid system whereupon it reacts with gaseous chlorine to produce the desired product composition enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine.
The initiator charge which is placed in the primary reactor to initiate the process of the present invention is defined as a liquid material which when contacted with gaseous chlorine reacts to produce hydrogen chloride. Although the requirement may be met with innumerable materials, as a practical matter, it is picoline charge and the recommended materials are chlorinated picoline mixture, preferably, a highly chlorinated picoline composition particularly of density 1.651.8. Such material would still contain reactable hydrogen but would avoid intro duction of foreign matter. It is to be noted that once the process has been initiated there will be a chlorinated pico- If no chlorinated picoline is available, a small amount of picoline diluted with an inert low boiling solvent may be employed, the solvent being readily removable from the product after recovery thereof. Introduction of several equivalents of anhydrous HCl prior to chlorine introduction is necessary in this case. Otherwise solid picoline monohydrochloride which is detrimental to good yields contemplated by the process of this invention will form.
The hydrogen chloride formed in situ is conducted to a cooled secondary reactor where under controlled temperated conditions it is contacted with picoline in an atmosphere of excess hydrogen chloride to form liquid picoline hydrochloride composition. It is to be noted that hydrogen chloride from an external source is not inoperable in this step but inasmuch as once the reaction has started theie is always an abundant internal supply of hydrogen chloride, a method which contemplates an external supply is impractical. In this step, initially, picoline hydrochloride is formed but in the presence of excess hydrogen chloride, a liquid composition is formed. The presence of excess hydrogen chloride and the smooth conversion of picoline to liquid picoline hydrochloride composition under controlled temperature conditions is critical and essential not only for obtaining good yields of the product but also for efiicient operation of the present invention. As will be discussed hereinafter in connection with .a production system suitable forcarryingout the present invention, an efiicient means for contacting hydrogen chloride and picoline is in a counter-current flow relationship and the smooth conduction of the resulting material to the primary reactor is achieved by down-flow of a liquid composition. The desired results are achieved by controlling the temperatures in such a manner that a significant proportion of the initial heat of reaction between picoline and hydrogen chloride is removed but wherein a sufficiency of heat is retained to permit the formation of a liquid composition and to maintain the composition in a liquid state along the down-flow path to the primary reactor. Achievement of desired temperature control is best accomplished by employing a reactorof such shape and/ or dimensions as to provide a high degree of positive temperature control throughout the reactor. Inasmuch as the reaction of picoline hydrochloride formation is exothermic, it is desirable that the reactor have a relatively large area of cooling surface or walls Where the extent of cooling may be externally controlled. A suitable temperature range for carrying out this step is from about 20 to about 70 C. It is essential that significantly higher temperatures be avoided in order that undersirable ,by-product formation or mechanical difiiculties resulting from such by-product formation be prevented. It is also important that temperatures appreciably below 20 C. be avoided to preclude mechanical difiiculties resulting from solid picoline hydrochloride separation or from chemical .difficulties resulting from solid picoline hydrochloride falling into or being carried into the primary reactor. It is important that solid picoline hydrochloride not be carried into the primary reactor. An average temperature of about 50 C. is convenient. It is also to be noted that unmodified picoline cannot be introduceddirectly into the primary reactor in place of the liquid compositionobtained as hereinabove described to achieve the same results. Such change will result in poor yields and frequently intractable mixtures.
The exact rate of introduction of chlorine into the primary reactor depends on the particular size of operation, shape of reactor, Whether or not mechanical mixing is employed, etc. For efiicient operation of this process, it is important that about 80 to 85 percent molar excess of chlorine be present at all times in the reactor to assure not only a rapid conversion of the reactant picolinehydrochloride material but also to continuously sweep out hydrogen chloride from the reactor. The desirablerate may be expressed in terms of the rate of introduction of the reactant picoline into the reaction system. Such rate is considered to be a ratioof chlorine to picoline of from about 11.521 to about 21.5:1 on weight basis. Illustrative of a desirable rate is-that of from-about 4 to 6 pounds of chlorine per hour at a picoline feed rate of 0.28 to 0.35 pounds per hour when introducedinto a, 6.4 gallon reactor containing about 4.5 gallons of reaction mixture. The
residence time is dependent on volume of reaction mixture and picoline feed rate necessary to hold a st ady state. By steady state is meant the condition attained when the composition of the reaction mixture is no longer changing significantly. The time necessary to achieve a steady state depends on conditions applied to the system andis readily determined by .the skilled in the art. The density of the reaction mixture at steady state is from about 10 to 12 pounds per gallon, the averagefigure being about 11 pounds per gallon. It is to be noted that this density is an average density of the overall mixture in the reactor inasmuch as there develops as the reaction approaches a steady state, a dual liquid phase system of substantially definite proportions and having the above average densities. The upper liquid phase is a liquid hydrochloride composition comprising picoline hydrochloride and lower chlorinated picoline hydrochloride in excess hydrogen chloride, and the lower liquid phase comprises a highly chlorinated mixture enriched in 3,4,5,6-tetra-.
chloro-2-(trichloromethyl)pyridine. Assuming the reactor charge composition set forth above, and a picoline feed rate of 0.3 pound per hour, and an average molecular weight of productof 300, the residence time would be hours.
It is further important in this process for the selective preparation of a mixture enriched in 3,4,5,6-tetrachloro-2- (trichloroznethyl)-pyridine that careful controls be made of the temperature of .the reaction mixture, i.e., the temperature of the primary reactor. It is critical and essential that the temperature not be allowed to remain over 120 C. for any significant period of time. The desired temperature range is from about to about 110 C. Consistently good results have been achieved at C.
The reaction may be carried out in the presence or absence of a catalytic light source. The use of irradiation is considered preferable. A light source emitting light at a wave length of from about 2000 A. to 5000 A. and particularly between about 3000 A. to about 4000 A. are suitable. When the reaction is carried out in the presence of light, the light source may double as a source of heat.
The reaction may be carried out in the presence or absence of a catalyst. A mixture enriched in highly chlorinated picoline compounds, particularly in 3,4,5,6- tetrachloro 2 (trichlorornethyl) pyridine is obtained in good yields in the absence of catalyst; this is noted particularly when product composition obtained by this method is compared with products obtained by using known chlorination methods. .However, it has been found that by using Lewis acid catalysts in the present process, the yield of the desired product composition is significantly increased; thus, the preferred method for preparing a mixture enriched in 3,4,5,6 tetrachloro-2-(trichloromethyl) pyridine contemplates the use of a Lewis acid catalyst. Any Lewis acid catalysts as understood in the art may be employed. Particularly desirable are aluminum chloride, phosphorus trichloride and ferric chloride. Others include stannic chloride, antimony trichloride, thionyl chloride, sulfuryl chloride, phosphorouspentachloride, calcium chloride, iodine, red phosphorus, etc. Lower valent salts of multi-valent metals as well as free metals may be employed. The latter when employed is readily converted by the hydrogen chloride formed in the reaction mixture to the corresponding metal chloride. The catalyst may be added in any amount up to 5 percent by weight of the picoline feed. Preferred amounts are from 0.5 to 1 percent by weight.
' The mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine thus obtained is water-white in color, has a substantially constant density, contains only minor proportions of lower chlorinated picolines and is substantially free of hydrogen chloride. This enriched product mixture forms a lower liquid phase in the reactor while the less chlorinated picoline dissolved in hydrogen chloride forms the less dense upper liquid phase. The exact composition of the product mixture to be removed from the reactor at the steady state may be determinedby vapor phase chromatographic analysis of samples or may be estimated by density comparison with a predetermined density-composition correlation. The average densities of the product enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, containing 3,4,5-trichloro-2-(trichloromethyl)pyridine and 3,4,5-trichloro-2-(dichloromethyl) pyridine as the major components vary from 1. 68 to 1.78,
usually about 1.73. The product may be bled from the reactor by conventional methods and may be separated into its components, if desired, by fractional distillation.
The present invention may be described more fully by reference to the accompanying flow sheet.
The apparatus comprises primarily of primary reactor A, reactor B, condenser C, hydrogen chloride absorption column D, chlorine drier E and gas shunting device F. Reactor A is the primary reactor to be employed as a liquid phase chlorinator; it is fitted with temperature control means a for heating or cooling and optionally with dimensions of reactor B are not important but must be such as to provide sufiicient cooling to prevent by-product formation but without excessive cooling as to cause separation of solid picoline hydrochloride. Good results have been obtained when the diameterzlength ratio was about 1:18 and tap water used for cooling. Condenser C has for its primary purpose avoidance of entrainment losses of reactant or product with effluent gases; it is fitted with cooling means d. A means for avoiding entrainment losses is necessary to obtain good yields contemplated by the method of the present invention; it is to be noted however that a separate condenser unit may not be necessary tinuously or periodically in portions. When the catalyst is introduced in the form'of a metal, it comes into contact with gaseous hydrogen chloride leaving reactor A, and is converted substantially immediately to the appropriate metal chloride. V
The following examples illustrate the inve'ntionbut are not'to be construed as limiting:
Example 1 An operation was carried out in an apparatus having a schematic arrangement set forth in the accompanying drawing wherein reactor A was a vessel of 17 liter capacity and illuminated with ultraviolet light, reactor 13 was a water-cooled column 2 inches in internal diameter and 36 inches in length, a condenser C was a water-cooled column 2 inches in diameter and 14 inches in length.
as shown in the diagram but may become part of an integral design of reactor B. Such modifications would be well-known to the skilled in the art. The hydrogen chloride absorption column D is a means for removing hydrogen chloride from the mixed chlorine-hydrogen chloride gases; it consists of downflowing water which meets the gases in counter-current relationship and aqueous hydrochloric acid is recovered at the bottom of the column. Chlorine drier B may be any suitable means for drying chlorine gas, a packed silica gel column being convenient; it is not by any means limited thereto and any device adapted to remove entrained water from chlorine using suitable dessicant such as sulfuric acid or magnesium perchlorate may be employed. A chlorine drier is of utmost importance in use of recycled chlorine inasmuch as the method of the present invention is carried out under substantially anhydrous conditions in contrast' to a single flow system.
As a first step in carrying out the reaction, an initiator charge, previously defined, is placed in reactor A. Chlorine gas is introduced into the thus charged reactor A at 1 whereupon a reaction takes place with the evolution of hydrogen chloride gas-which leaves the reactor through inlet-outlet 2 and proceeds upward through orifice 4 into reactor B. Picoline is introduced at inlet 6 where it proceeds by gravity fiow into cooled reactor B, meeting the hydrogen chloride in a counter-current flow relationship and reacting on the walls thereof to form picoline hydrochloride which in the presence of excess hydrogen chloride is converted into a liquid picoline hydrochloride composition. the down-flowing liquid picoline hydrochloride composi- The temperature in reactor B is controlled so that Reactor A was charged with 3.2 pounds of a mixture of partially chlorinated picoline from a previous run as the initiator charge. The temperature of the charged reactor was then raised to 100 C. and gaseous chlorine introduced at inlet 1 at arate of about 9 pounds per-hour. The gaseous chlorine reacted with the partially chlorinated picoline in the initiator charge, forming hydrogen chloride which evolved from the mixture, leaving reactor A at 2 and entering reactor B at 4. Picoline was introduced at inlet 6 at a rate of 0.7 pound per hour. The picoline, thus introduced, contacted hydrogen chloride gas in a counter-current flow relationship and reacted therewith forming picoline hydrochloride which in the presence of excess hydrogen chloride gas formed a liquid picoline hydrochloride composition which proceeded downward into the primary reactor. 0.5 pound of aluminum chloride catalyst (about 1 percent by weight based on the total picoline used) was introduced at inlet 3. The catalyst came into contact with the liquid picoline'hydrochlorine composition leaving reactor B and was carried therewith into reactor A. The liquid picoline hydrochloride composition thus continuously introduced into the chlorination medium of reactor A, reacted with gaseous chlorine which was continuously introduced over a period of 72 hours to produce a product mixture enriched in 3,4,5,6- tetrachloro-Z-(trichloromethyl)pyridine. After the steady state was reached, the product mixture was continuously removed from the reactor at 7 and amounted to 130 pounds. Vapor phase chromatographic analysis of the product mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl) pyridine showed the mixture to contain in adtion remains homogeneous and continues smoothly without the separation of solid picoline hydrochloride on the walls of the apparatus. The liquid picoline hydrochloride composition enters reactor A where, in the liquid phase and under controlled temperature conditions, it reacts with gaseous chlorine to produce the desired product mixture of chlorinated picolines enriched in 3,4,5,6-tetrachloro-2 (trichloromethyl) pyridine which may be recovered at 7.
Hydrogen chloride, chlorine gas and entrained liquids proceed from reactor B to condenser C where the entrained liquids are separated from the gases by condensation and returned to reactor B. The gases proceed from the condenser to absorption column D where the gases meet down-flowing water in a counter-current relationship and wherein hydrogen chloride dissolves in the water forming hydrochloric acid which is recovered at 8. The gaseous chlorine proceeds from the absorption column at 9 and proceeds to chlorine drier E. The chlorine after passing through drying column B is joined at F with fresh chlorine and recycled through the reactor system.
When the process of the present invention is carried out in the presence of a catalyst, the catalyst may be introduced at inlet 3,'whereby it is conveyed into reactor A through inlet-outlet 2. The catalyst may be added condition 3,4,5-trichloro-2-(trichloromethyDpyridine and 3, 4,5-trichloro-2-(dichloromethyl)pyridine as major components. The product composition in mole percent wasas follows: 30 percent 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 32 percent 3,-4,5-trichloro-2-(trichloromethyl)pyridine, 16 percent 3,4,5-trichloro-2-(dichloromethyl)pyridine, about 6 percent 3,5-dichl0ro-2-(trichloromethyl) pyridine, about 7 percent 3,5,6-trichloro-2-(trichloromethyl) pyridine and about 4 percent 3,5-dichloro- Z-(dichloromethyl)pyridine.
The components of the reaction mixture are readily separated by fractional distillation. On distilling product mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, i.e., mixture containing primarily 3,4,5, 6- tetrachloro-2-(trichloromethyl)pyridine, 3,4,5-trichloro-2- trichloromethyl) pyridine and 3,4,5-trichloro-2-(dichloromethyl)pyridine, it is found that the lower chlorinated products distill ofl? in the forerun, 3,4,5-trichloro-2-(dichloromethyl) pyridine distills at from to C. at 1 millimeter of mercury pressure, 3,4,5-trichloro-2-(trichloromethyl-)pyridine at from 172 to 175 C. at 25 millimeters of mercury pressure and 3,4,5J6-tetrachloro- 2-(trichloromethyl) pyridine is recovered as residue which solidifies on cooling and melts at 58 60 C. after recrystallization from carbon tetrachloride.
Example 2 A reaction was carried out in a manner substantially as I percent troduced in the form of aluminum turnings, said aluminum reacting with the hydrogen chloride evolved from reactor A to form aluminum chloride in situ. By this modified procedure there was obtained 32 mole percent 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 30 mole 3,4,5-trichloro-2-(trichloromethyl)pyridine and 15 mole percent 3,4,5-trichloro-2-(dichloromethyl)pyridine.
Example 3 A similar operation was carried out in which the following modifications were made (a) change in rate of introduction of picoline to 250 grams per hour, (b) dark reaction, i.e., ultraviolet light was not employed, and (c) change in amount of catalyst employed (2 percent by weight of aluminum based on weight of picoline used). In a manner previously described, the chlorination was allowed to proceed for 40 hours to obtain a product mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl) pyridine which was continuously recovered from the reactor. Vapor phase chromatographic analysis of the product mixture showed 29 mole percent of 3,'4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 33 mole percent of 3,4,5-trichloro-2-(trichloromethyl)pyridine and 15 mole percent of 3,4,5-trichloro-2-(dichloromethyl) pyridine.
Example 4 In another similar operation, an irradiated chlorination was carried out wherein ferric chloride catalyst, introduced as metallic iron in an amount of 1.5 percent by weight of picoline, was employed. The reaction was carried out in a manner as previously described by introducing chlorine gas into reactor A charged with a partially chlorinated picoline mixture and introducing picoline into reactor B at a rate of 250 grams per hour for 24 hours to obtain a highly chlorinated product composition containing 29 mole percent 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 32 mole percent 3,4,5-trichloro-2-(trichlorornethyl) pyridine and 17 mole percent 3,4,5-trichloro-2- dichlorornethyl) pyridine.
' Example In another operation, picoline was introduced into reactor B at a rate of 250 grams per hour for 30 hours, phosphorus pentachloride catalyst was added to reactor A in an amount totalling 1 percent of the amount of total picoline employed, and gaseous chlorine was bubbled into an irradiated mixture of initiator charge of partially chlorinated picolines in reactor A for a period of 30 hours to obtain product containing 30 percent of 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine, 33 percent of 3,4,5- trichloro-Z-(trichloromethyl)pyridine and 17 percent of 3,4,5-trichloro-2-(dichloromethyDpyridine.
The process of the present invention produces a very highly useful product composition which may be employed without change or may be separated into major components for ultimate use in product compositions or as starting materials for the preparation of other desirable products. Thus the 3,4,5,6 tetrachloro 2 (trichloromethyl)pyridine enriched product may be diluted with inert adjuvants to obtain pesticidal treating compositions. In such use, the product is mixed with dispersing agents and dispersed in water to obtain spray compositions which when applied to foliage of bean, pigweed and foxtail plants effect complete kills of said plants. Alternatively, the 3,4,5,6-tetrachloro-2-(trichloromethyl)pyridine enriched product may be distilled to recover 3,4,5,6- tetrachloro-Z-(trichloromethyl)pyridine or 3,4,5-trichloro-2-(trichloromethyl)pyridine which may separately be employed in pesticidal compositions. The product mixture may also be distilled to recover the components which may be employed as intermediates in the preparation of other chemical compounds, such as for example, aminochloropyridine compounds by heating the recovered component with liquid ammonia in a sealed vessel at temperatures of from about 70 to above 190 C. at autogeneous pressure. The resulting aminochloropyridine compounds may be employed for the control of insect pests such as house-fly, cockroach, mites, aphids, etc. or for the eradication of weeds or weed seeds. In such applications, the aminochloropyridine compounds may be prepared with dispersing agents to form aqueous dispersion or dispersed on inert solids to form dust compositions to be applied to infested areas.
We claim:
1. A process for preparing a mixture enriched in 3,4.5,6 tetrachloro 2 (trichloromethyl) pyridine which comprises (1) contacting (X-PiCOline and hydrogen chloride in a cooled reactor at temperatures in the range of from about 20 C. to about 70 C. to produce a liquid tx-picoline hydrochloride composition,
(2) contacting in the liquid phase in the absence of added water at temperatures in the range of from about C. to about 120 C., said liquid tit-picoline hydrochloride composition and gaseous chlorine;
wherein in the foregoing process, the chlorine and OL- picoline are introduced in a ratio of chlorine to picoline of from about 11.511 to about 21.5:1 on a weight basis.
2. A process for preparing a mixture enriched in 3,4,5,6 tetrachloro 2 (trichloromethyl)pyri-dine which comprises (1) contacting LZ-PiCOiine and hydrogen chloride at temperatures in the range of from about 20 C. to 70 C. to produce a liquid a-picoline hydrochloride composition,
(2) contacting said liquid OL-PiCOilH6 hydrochloride composition with gaseous chlorine in the liquid phase in the absence of added water at temperatures in the range of from about 95 C. to about C.;
wherein in the foregoing process, the chlorine and a-picoline are introduced in a ratio of chlorine to picoline of from about ll.5:1 to 21.5:1 on a weight basis.
3. A method according to claim 2 wherein step (2) is carried out while the mixture is irradiated with actinic radiation.
4. A method according to claim 2 wherein step (2) is carried out in the presence of a Lewis acid catalyst.
5. A method according to claim 2 wherein step (2) is carried out in the presence of Lewis catalyst and actinic radiation.
6. A continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichlorornethyl)- pyridine which comprises (1) continuously feeding tat-picoline into a cooled reactor,
(2) contacting substantially instantaneously at temperatures in the range of from about 20 C. to about 70 C. in said reactor, said OL-PlCOilflfi and hydrogen chloride to produce a liquid ot-picoline hydrochloride composition,
(3) conducting said liquid tx-picoline hydrochloride composition from said cooled reactor to a controlled heated reactor,
(4) continuously feeding gaseous chlorine into said heated reactor and contacting therein in the liquid phase in the absence of added water at temperatures of from about 95 C. to about C. for time sufficient to complete the reaction, the chlorine and liquid picoline hydrochloride composition;
wherein in the foregoing process, the chlorine and apicoline are introduced in a ratio of chlorine to picoline of from about 11.5:1 to about 21.5:1 on a weight basis.
7. A continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)- pyridine which comprises (1) charging a heated reactor with a picoline charge,
(2) continuously passing gaseous chlorine therethrough to produce gaseous hydrogen chloride,
' (3) conducting gaseous hydrogen chloride from the heated reactor to a cooled reactor,
(4) continuously feeding a-picoline into a cooled reactor to contact and react with hydrogen chloride at temperatures in the range of from about 20 C. to about 70 C. to form a liquid picoline hydrochloride composition,
( conducting the liquid a-picoline hydrochloride composition to the heated reactor maintained in the temperature range offrom about 95 C. to about 120 C. to react with chlorine in the liquid phase in the absence of added water to produce the desired product composition enriched in 3,4,5,6-tetrachloro-2-( trichloromethyl) pyridine,
(6) continuously withdrawing the latter from the reaction mixture;
wherein in the foregoing process, the chlorine and apicoline are introduced in a ratio of chlorine to picoline of from about 11.5 :1 to about 21.5 :1 on a weight basis.
8. A continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyl)- pyridine which comprises 1) charging a heated reactor with a picoline charge comprising chlorinated picolines having a density of from about 1.65 to 1.8,
(2) continuously passing gaseous chlorine through to produce gaseous hydrogen chloride,
(3) conducting gaseous hydrogen chloride from the heated reactor to a cooled reactor,
(4) continuously feeding OL-PiCOllHe into a cooled reactor to contact and react with hydrogen chloride at temperatures in the range of from about 20 C. to
- about 70 C. to form a liquid a-picoline hydrochloride composition,
(5) conducting the liquid a-picoline hydrochloride composition to the heated reactor maintained in the temperature range of fromabout 95 C. to about 120 C. to react with the gaseous chlorine in the liquid phase in the absence of added water to produce the desired product composition enriched in 3,4,5',6- tetrachloro-2- trichloromethyl pyridine,
(6) continuously withdrawing the latter from the reaction mixture;
wherein in the foregoing process, the chlorine and apicoline are introduced in a ratio of chlorine to picoline of from about 11.5:1 to about 21.5:1 on a weight basis.
9. A process for preparing a mixture enriched in 3,4,5,6 tetrachloro 2-(trichloromethyl)pyridine which comprises (1) contacting a-picoline and hydrogen chloride in a cooled reactor at temperatures in the range of from about 20 C. to about 70 C. to produce a liquid orpicoline hydrochloride composition,
(2) contacting in the liquid phase in the absence of added water at temperatures in the range of from about 95 C. to about 120 C., said liquid a-picoline hydrochloride composition and gaseous chlorine:
wherein in the foregoing process, the rate of introduction of chlorine into the reactor is such as to provide therefor its presence therein throughout the reaction in about 80 to 85 percent molar excess on a stoichiometric basis.
10. A process for preparing a mixture enriched in 3,4,5,6 tetrachloro '2-(trich-loromethyl)pyridine which comprises i (1) contacting a-picoline and hydrogen chloride at temperatures in the range of from about 20 C. to about 70 C. to produce a liquid a-picoline hydrochloride composition,
(2) contacting said liquid a-picoline hydrochloride composition with gaseous chlorine in the liquid phase in the absence of added water at temperatures in the range of from about 95 C. to about 105 C;
wherein in the foregoing process, the rate of introduction of chlorine into the retactor is such as to provide for its presence therein throughout the reaction in about 80 to 85 percent molar excess on a stoichiomet-ric basis.
11. A method according to claim 10 wherein step (2) is carried out while the mixture is irradiated with actinic radiation.
12. A method according to claim 10 wherein step (2) is carried out in the presence of a Lewis acid catalyst.
13. A method according to claim 10 wherein step (2) is carried out in the presence or Lewis acid catalyst and actinic radiation.
14. A continuous process :for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichlorome-thyl) pyridine which comprises (1) continuously feeding a-picoline into a cooled r actor, I
(2) contacting substantially instantaneously at temperatures in the range OflfIOlTl about 20 C. to about C. in said reactor, said a-p-icoline and hydrogen chloride to produce a liquid a-picoline hydrochloride composition,
(3) conducting said liquid a-picoline hydrochloride composition from said cooled reactor to a controlled heated reactor, v
(4) continuously feeding gaseous chlorine into said heated reactor and contacting therein in the liquid phase in the absence of added water at temperatures of firom about 95 C. to about 120 C. for time sufficient to complete the reaction, the chlorine and liquid picoline hydrochloride composition;
wherein in the foregoing process, the rate of introduction of chlorine into the reactor is such as to provide for its presence therein throughout the reaction in about to percent molar excess on a stoichiometric basis.
15. A continuous process for the preparation of a mixture enriched in 3,4,5,6 -tetrachloro-2-(trichloromethyl)pyridine which comprises (1) charging a heated reactor with a picoline charge,
(2) continuously passing gaseous chlorine therethrough to produce gaseous hydrogen chloride,
(3) conducting gaseous hydrogen chloride from the heated reactor to a cooled reactor,
(4) continuously feeding a-picoline into a cooled reactor to contact and react with hydrogen chloride at temperatures in the range of from about 20 C. to about 70 C. to form a liquid picoline hydrochloride composition,
(5) conducting the liquid a-picoline hydrochloride composition to the heated reactor maintained in the temperature range of from about C. to about C. to react with chlorine in the liquid phase in the absence of added water to produce the desired product composition enriched in 3,4,5,6-tetrachloro-2- trichloromethyl pyridine,
(6) continuously withdrawing the latter from the reaction mixture;
wherein in the foregoing process, the rate'of introduction of chlorine into the reactor is such as to provide for its presence therein throughout the reaction in about 80 to 85 percent molar excess on a stoichiometric basis.
16. A continuous process for the preparation of a mixture enriched in 3,4,5,6-tetrachloro-2-(trichloromethyDpy ridine which comprises (1) charging a heated reactor with a picoline charge comprising chlorinated picolines having a density of from about 1.65 to 1.8,
(2) continuously passing gaseous chloride therethrough to produce gaseous hydrogen chloride; (3) conducting gaseous hydrogen chloride from the heated reactor to a cooled reactor,
(4) continuously feeding ocpiCO-ll116 into a cooled reactor to contact and react with hydrogen chloride at temperatures in the range of from about 20 C. to about 70 C. to form a liquid a-picoline hydrochloride composition,
(5) conducting the liquid a-picoline hydrochloride composition to the heated reactor maintained in the eer e-i 1 1 12 temperature range of from -about.95 C. to about OTHER REFERENCES 2 to react w the 8-2 9 chlorme the K-lingsberg: fPyridine and Derivatives, pt. 2, pp. 303 liquid phase in the absence of added water to pro- 5 (196.1% 1 the ldesirsd Product COmPQSiIiQII enriched in .McBee et aLLInd. and Eng. Chem, vol. 39, pp. 3,8991 3,4,5,6-te'tiraehloro 2 (trichloromethyl pyridine. 5 (1947) o nu u Withdrawing the latter from the Sell: J. Chem. Soc., vol. 93, pp. 1993-5 1908).
action t Wibaut et aL: Rec. trav. chim., vol. 58, pp. 709-721 wherein in the foregoing process, the rate of introduc- 1939 tion of chlorineinto t-he reactoris such as to provide for its presence therein throughout the reaction in about 80 10 JOHN H. MACK, Primary Exmniner.
to 85 percent molar excess on a stoich-iornetric basis. DUVAL T. MCCUTCHEN, JOHN D RANDOLPH References Cited by the Examiner m UNITED STATES PATENTS 2,679,453 5/1954 Brett et ai. 26029O X B4. W. WESTERN, H. S. WILLIAMS, 15 Assistant Examiners.
Claims (2)
- 2. A PROCESS FOR PREPARING A MIXTURE ENRICHED IN 3,4,5,6-TETRACHLORE-2-(TRICHLOROMETHYL)PYRIDINE WHICH COMPRISES (1) CONTACTING A-PICOLINE AND HYDROGEN CHLORIDE AT TEMPERATURES IN THE RANGE OF FROM ABOUT 20*C. TO 70*C. TO PRODUCE A LIQUID A-PICOLINE HYDROCHLORIDE COMPOSITION, (2) CONTACTING SAID LIQUID A-PICOLINE HYDROCHLORIDE COMPOSITION WITH GASEOUS CHLORINE IN THE LIQUID PHASE IN THE ABSENCE OF ADDED WATER AT TEMPERATURES IN THE RANGE OF FROM ABOUT 95*C. TO ABOUT 105*C.; WHEREIN IN THE FOREGOING PROCESS, THE CHLORINE AND A-PICOLINE ARE INTRODUCED IN A RATIO OF CHLORINE TO PICOLINE OF FROM ABOUT 11:5 TO 21.5:1 ON A WEIGHT BASIS.
- 3. A METHOD ACCORDING TO CLAIM 2 WHEREIN STEP (2) IS CARRIED OUT WHILE THE MIXTURE IS IRRADIATED WITH ACTINIC RADIATION.
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4483993A (en) * | 1983-04-08 | 1984-11-20 | Kalama Chemical, Inc. | Production of polychlorinated pyridine mixtures by liquid phase chlorination of beta-picoline or beta-picoline hydrochloride |
US4487935A (en) * | 1982-09-24 | 1984-12-11 | Kalama Chemical, Inc. | Production of mixtures rich in 6-chloro-2-trichloromethyl pyridine |
US4517369A (en) * | 1982-09-29 | 1985-05-14 | Kalama Chemical, Inc. | Preparation of mixtures rich in 3,4,5,6-tetrachloro-2-trichloromethyl pyridine |
US4564681A (en) * | 1982-09-24 | 1986-01-14 | Kalama Chemical, Inc. | Production of mixtures rich in 3-chloro-2-trichloromethyl pyridine |
US4577027A (en) * | 1982-09-24 | 1986-03-18 | Kalama Chemical, Inc. | Production of polychlorinated pyridine mixtures by direct liquid phase chlorination of alpha-picoline |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2679453A (en) * | 1952-10-10 | 1954-05-25 | Charles H Brett | Method and composition for the control of undesired vegetation |
-
0
- US US3256167D patent/US3256167A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2679453A (en) * | 1952-10-10 | 1954-05-25 | Charles H Brett | Method and composition for the control of undesired vegetation |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4487935A (en) * | 1982-09-24 | 1984-12-11 | Kalama Chemical, Inc. | Production of mixtures rich in 6-chloro-2-trichloromethyl pyridine |
US4564681A (en) * | 1982-09-24 | 1986-01-14 | Kalama Chemical, Inc. | Production of mixtures rich in 3-chloro-2-trichloromethyl pyridine |
US4577027A (en) * | 1982-09-24 | 1986-03-18 | Kalama Chemical, Inc. | Production of polychlorinated pyridine mixtures by direct liquid phase chlorination of alpha-picoline |
US4517369A (en) * | 1982-09-29 | 1985-05-14 | Kalama Chemical, Inc. | Preparation of mixtures rich in 3,4,5,6-tetrachloro-2-trichloromethyl pyridine |
US4483993A (en) * | 1983-04-08 | 1984-11-20 | Kalama Chemical, Inc. | Production of polychlorinated pyridine mixtures by liquid phase chlorination of beta-picoline or beta-picoline hydrochloride |
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